Erbe USA Inc recalls Flexible Cryoprobe (OD 2.4mm, L1.15mm) REF: 20402-411. For surgical use
- Recall date
- February 12, 2026
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1568-2026
- FDA classification
- Class I
- Brand / firm
- Erbe USA Inc
- Sold / distributed
- US Nationwide distribution, including Puerto Rico.
Why it was recalled
Probes may rupture/burst during activation
Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.
What was recalled
Flexible Cryoprobe (OD 2.4mm, L1.15mm) REF: 20402-411. For surgical use
Get recall alerts
Free email alert whenever Erbe USA Inc has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Erbe USA Inc